"Electroencephalography" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Recording of electric currents developed in the brain by means of electrodes applied to the scalp, to the surface of the brain, or placed within the substance of the brain.
| Descriptor ID |
D004569
|
| MeSH Number(s) |
E01.370.376.300 E01.370.405.245
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Electroencephalography".
Below are MeSH descriptors whose meaning is more specific than "Electroencephalography".
This graph shows the total number of publications written about "Electroencephalography" by people in this website by year, and whether "Electroencephalography" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2006 | 1 | 0 | 1 |
| 2007 | 0 | 1 | 1 |
| 2010 | 1 | 1 | 2 |
| 2011 | 0 | 1 | 1 |
| 2012 | 0 | 1 | 1 |
| 2013 | 0 | 2 | 2 |
| 2015 | 0 | 1 | 1 |
| 2018 | 0 | 1 | 1 |
| 2021 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Electroencephalography" by people in Profiles.
-
Novel KCNH1 Mutations Associated with Epilepsy: Broadening the Phenotypic Spectrum of KCNH1-Associated Diseases. Genes (Basel). 2021 01 21; 12(2).
-
The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant. Ann Neurol. 2018 05; 83(5):926-934.
-
CHD2 variants are a risk factor for photosensitivity in epilepsy. Brain. 2015 May; 138(Pt 5):1198-207.
-
Mutation in the mitochondrial tRNA(Ile) gene causes progressive myoclonus epilepsy. Seizure. 2013 Jul; 22(6):483-6.
-
Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy. Epilepsia. 2013 Feb; 54(2):256-64.
-
Schizophrenia risk polymorphisms in the TCF4 gene interact with smoking in the modulation of auditory sensory gating. Proc Natl Acad Sci U S A. 2012 Apr 17; 109(16):6271-6.
-
AIMP1/p43 mutation and PMLD. Am J Hum Genet. 2011 Mar 11; 88(3):391; author reply 393-5.
-
Association of a rare variant with mismatch negativity in a region between KIAA0319 and DCDC2 in dyslexia. Behav Genet. 2011 Jan; 41(1):110-9.
-
Anti-N-methyl-D-aspartate-receptor encephalitis in a four-year-old girl. J Pediatr. 2010 Feb; 156(2):332-4.
-
Subfield-specific loss of hippocampal N-acetyl aspartate in temporal lobe epilepsy. Epilepsia. 2008 Jan; 49(1):40-50.
MeSH information
